EventsThe 11th International Electronic Conference on Synthetic Organic Chemistry
Published
This submission belongs to the session e. Symposium on Microwave Assisted Synthesis of the event The 11th International Electronic Conference on Synthetic Organic Chemistry
Published date
30 Nov, 2007
Citation
Sachin S. Laddha, Satayendra P. Bhatnagar, Efficient Niementowski synthesis of novel derivatives of 1,2,9,11-tetrasubstituted-7H-thieno[2',3':4,5]pyrimido[6,1-b]-quinazolin-7-one, in Proceedings of The 11th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2007, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-11-01351
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Efficient Niementowski synthesis of novel derivatives of 1,2,9,11-tetrasubstituted-7H-thieno[2',3':4,5]pyrimido[6,1-b]-quinazolin-7-one

Satayendra P. Bhatnagar 1
1. Department of Pharmaceutical Sciences, Birla Institute of Technology, Mesra, Ranchi, India
Abstract
Starting Starting from 5,6-disubstituted-3H-thieno[2,3-d]pyrimidin-4-ones, novel 1,2,9,11-tetrasubstituted-7H-thieno[2',3':4,5]pyrimido[6,1-b]quinazolin-7-ones could be reached in two steps through a von Niementowski reaction, which involves condensation of substituted anthranilic acids with a 4-chloro-5,6-disubstituted-3H-thieno[2,3-d] pyrimidines. Microwave irradiation in acetic acid media was used in order to improve reactions where conventional heating was limited.
Keywords
cyclization
fused thieno-[2,3-d]-pyrimidine
Microwave assisted synthesis
Sulphur heterocycles
Expedite regioselective synthesis of pyrimidobenzimidazoles
A Novel Microwave Synthesis of Unsubstituted Cyclic Imides